FDA applicant

Infra-Med Technologies, Inc.

Flower Mound, TX1 decision2000–20000 recalls

FDA records 1 decision for Infra-Med Technologies, Inc. (Flower Mound, TX) in 2000: 1 510(k) clearance. All are in product code LDQ (Unnamed device). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Infra-Med Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Infra-Med Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Infra-Med Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Infra-Med Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?